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Journal Abstract Search
138 related items for PubMed ID: 8490057
1. Biochemical diagnosis of a fatal case of Günther's disease in a newborn with hydrops foetalis. Verstraeten L, Van Regemorter N, Pardou A, de Verneuil H, Da Silva V, Rodesch F, Vermeylen D, Donner C, Noël JC, Nordmann Y. Eur J Clin Chem Clin Biochem; 1993 Mar; 31(3):121-8. PubMed ID: 8490057 [Abstract] [Full Text] [Related]
2. Porphyrins in urine, plasma, erythrocytes, bile and faeces in a case of congenital erythropoietic porphyria (Gunther's disease) treated with blood transfusion and iron chelation: lack of benefit from oral charcoal. Gorchein A, Guo R, Lim CK, Raimundo A, Pullon HW, Bellingham AJ. Biomed Chromatogr; 1998 Mar; 12(6):350-6. PubMed ID: 9861496 [Abstract] [Full Text] [Related]
3. Interdependence between degree of porphyrin excess and disease severity in congenital erythropoietic porphyria (Günther's disease). Freesemann AG, Bhutani LK, Jacob K, Doss MO. Arch Dermatol Res; 1997 Apr; 289(5):272-6. PubMed ID: 9164637 [Abstract] [Full Text] [Related]
4. Congenital Erythropoietic Porphyria: A Rare Case of Photosensitivity with Hemolytic Anaemia and Mental Retardation. Shirazi N, Chauhan P, Jindal R, Ahmad S. J Coll Physicians Surg Pak; 2019 Jun; 29(6):S23-S25. PubMed ID: 31142411 [Abstract] [Full Text] [Related]
5. Bullous skin lesions in a jaundiced infant after phototherapy: a case of congenital erythropoietic porphyria. Baran M, Eliaçık K, Kurt I, Kanık A, Zengin N, Bakiler AR. Turk J Pediatr; 2013 Jun; 55(2):218-21. PubMed ID: 24192686 [Abstract] [Full Text] [Related]
6. Congenital erythropoietic porphyria (Günther's disease): two cases with very early prenatal manifestation and cystic hygroma. Pannier E, Viot G, Aubry MC, Grange G, Tantau J, Fallet-Bianco C, Muller F, Cabrol D. Prenat Diagn; 2003 Jan; 23(1):25-30. PubMed ID: 12533808 [Abstract] [Full Text] [Related]
7. Severe Perinatal Presentations of Günther's Disease: Series of 20 Cases and Perspectives. Goudet C, Ged C, Petit A, Desage C, Mahe P, Salhi A, Harzallah I, Blouin JM, Mercie P, Schmitt C, Poli A, Gouya L, Barlogis V, Richard E. Life (Basel); 2024 Jan 17; 14(1):. PubMed ID: 38255745 [Abstract] [Full Text] [Related]
8. Neonatal hemolytic anemia does not always indicate thalassemia: a case report. Al-Harazi AA, Al-Eryani BM, Al-Sharafi BA. BMC Res Notes; 2017 Sep 12; 10(1):476. PubMed ID: 28899405 [Abstract] [Full Text] [Related]
9. [Gunther's congenital erythropoietic porphyria in an 8-month old girl (author's transl)]. Mascaro-Galy C, Mascaro JM, Albero F. Ann Dermatol Venereol; 1977 Jan 12; 104(1):32-7. PubMed ID: 843024 [Abstract] [Full Text] [Related]
10. Ocular involvement in two symptomatic congenital erythropoietic porphyria. Oguz F, Sidal M, Bayram C, Sansoy N, Hekim N. Eur J Pediatr; 1993 Aug 12; 152(8):671-3. PubMed ID: 8404971 [Abstract] [Full Text] [Related]
11. [Allogeneic bone marrow transplantation in congenital erythropoietic porphyria. Gunther's disease]. Lagarde C, Hamel-Teillac D, De Prost Y, Blanche S, Thomas C, Fischer A, Nordmann Y, Ged C, De Verneuil H. Ann Dermatol Venereol; 1998 Feb 12; 125(2):114-7. PubMed ID: 9747227 [Abstract] [Full Text] [Related]
12. Successful cord blood stem cell transplantation for congenital erythropoietic porphyria (Gunther's disease). Zix-Kieffer I, Langer B, Eyer D, Acar G, Racadot E, Schlaeder G, Oberlin F, Lutz P. Bone Marrow Transplant; 1996 Jul 12; 18(1):217-20. PubMed ID: 8832020 [Abstract] [Full Text] [Related]
13. A rare cause of fetal ascites: A case report of Günther's disease. Lienhardt A, Aubard Y, Laroche C, Gilbert B, Bernard P, Massri K, Bouleisteix J. Fetal Diagn Ther; 1999 Jul 12; 14(5):257-61. PubMed ID: 10529564 [Abstract] [Full Text] [Related]
14. Congenital erythropoietic porphyria: prenatal diagnosis and autopsy findings in two sibling fetuses. Daïkha-Dahmane F, Dommergues M, Narcy F, Gubler MC, Dumez Y, Gauthier E, Nordmann Y, Nessmann C, Terrasse G, Muller F. Pediatr Dev Pathol; 2001 Jul 12; 4(2):180-4. PubMed ID: 11178635 [Abstract] [Full Text] [Related]
15. [Congenital erythropoietic porphyria. Apropos of a fatal case in the neonatal period due to acute hemolysis with hepatic failure]. de Verneuil H, Moreau-Gaudry F, Ged C, Bensidhoum M, Hombrados I, Tricoire J, Rolland M. Arch Pediatr; 1995 Aug 12; 2(8):755-61. PubMed ID: 7550841 [Abstract] [Full Text] [Related]
16. Congenital erythropoietic porphyria: clinical, biochemical, and enzymatic profile of a severely affected infant. Huang JL, Zaider E, Roth P, Garcia O, Pollack S, Poh-Fitzpatrick MB. J Am Acad Dermatol; 1996 May 12; 34(5 Pt 2):924-7. PubMed ID: 8621830 [Abstract] [Full Text] [Related]
17. Non-immune hydrops fetalis and bilateral pulmonary hypoplasia in a newborn infant with extralobar pulmonary sequestration. Brus F, Nikkels PG, van Loon AJ, Okken A. Acta Paediatr; 1993 Apr 12; 82(4):416-8. PubMed ID: 8318813 [Abstract] [Full Text] [Related]
18. Adult-onset congenital erythropoietic porphyria (Günther's disease) presenting with thrombocytopenia. Murphy A, Gibson G, Elder GH, Otridge BA, Murphy GM. J R Soc Med; 1995 Jun 12; 88(6):357P-358P. PubMed ID: 7629774 [Abstract] [Full Text] [Related]
19. Dual porphyria of coexisting variegata and cutanea tarda. Sieg I, Bhutani LK, Doss MO. Eur J Clin Chem Clin Biochem; 1995 Jul 12; 33(7):405-10. PubMed ID: 7548446 [Abstract] [Full Text] [Related]